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Mutation screening of EXT1 and EXT2 by denaturing high-performance liquid chromatography, direct sequencing analysis, fluorescence in situ hybridization, and a new multiplex ligation-dependent probe amplification probe set in patients with multiple osteochondromas.
Jennes I, Entius MM, Van Hul E, Parra A, Sangiorgi L, Wuyts W. Jennes I, et al. Among authors: sangiorgi l. J Mol Diagn. 2008 Jan;10(1):85-92. doi: 10.2353/jmoldx.2008.070086. Epub 2007 Dec 28. J Mol Diagn. 2008. PMID: 18165274 Free PMC article.
Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome.
Bowen ME, Boyden ED, Holm IA, Campos-Xavier B, Bonafé L, Superti-Furga A, Ikegawa S, Cormier-Daire V, Bovée JV, Pansuriya TC, de Sousa SB, Savarirayan R, Andreucci E, Vikkula M, Garavelli L, Pottinger C, Ogino T, Sakai A, Regazzoni BM, Wuyts W, Sangiorgi L, Pedrini E, Zhu M, Kozakewich HP, Kasser JR, Seidman JG, Kurek KC, Warman ML. Bowen ME, et al. Among authors: sangiorgi l. PLoS Genet. 2011 Apr;7(4):e1002050. doi: 10.1371/journal.pgen.1002050. Epub 2011 Apr 14. PLoS Genet. 2011. PMID: 21533187 Free PMC article.
Heparin-like heparan sulfate from rabbit cartilage.
Parra A, Veraldi N, Locatelli M, Fini M, Martini L, Torri G, Sangiorgi L, Bisio A. Parra A, et al. Among authors: sangiorgi l. Glycobiology. 2012 Feb;22(2):248-57. doi: 10.1093/glycob/cwr143. Epub 2011 Sep 20. Glycobiology. 2012. PMID: 21933839
117 results